Suppr超能文献

将微量注射靶向发育中的非洲爪蟾肾脏的技术。

Technique to Target Microinjection to the Developing Xenopus Kidney.

作者信息

DeLay Bridget D, Krneta-Stankic Vanja, Miller Rachel K

机构信息

Department of Pediatrics, Pediatric Research Center, University of Texas McGovern Medical School.

Department of Pediatrics, Pediatric Research Center, University of Texas McGovern Medical School; Program in Genes & Development, University of Texas Graduate School of Biomedical Sciences.

出版信息

J Vis Exp. 2016 May 3(111):53799. doi: 10.3791/53799.

Abstract

The embryonic kidney of Xenopus laevis (frog), the pronephros, consists of a single nephron, and can be used as a model for kidney disease. Xenopus embryos are large, develop externally, and can be easily manipulated by microinjection or surgical procedures. In addition, fate maps have been established for early Xenopus embryos. Targeted microinjection into the individual blastomere that will eventually give rise to an organ or tissue of interest can be used to selectively overexpress or knock down gene expression within this restricted region, decreasing secondary effects in the rest of the developing embryo. In this protocol, we describe how to utilize established Xenopus fate maps to target the developing Xenopus kidney (the pronephros), through microinjection into specific blastomere of 4- and 8-cell embryos. Injection of lineage tracers allows verification of the specific targeting of the injection. After embryos have developed to stage 38 - 40, whole-mount immunostaining is used to visualize pronephric development, and the contribution by targeted cells to the pronephros can be assessed. The same technique can be adapted to target other tissue types in addition to the pronephros.

摘要

非洲爪蟾(青蛙)的胚胎肾,即前肾,由单个肾单位组成,可作为肾脏疾病的模型。非洲爪蟾胚胎体积大,在体外发育,并且可以通过显微注射或外科手术轻松操作。此外,已经建立了早期非洲爪蟾胚胎的命运图谱。对最终将发育为感兴趣器官或组织的单个卵裂球进行靶向显微注射,可用于在该受限区域内选择性地过表达或敲低基因表达,减少发育中胚胎其他部分的次要影响。在本方案中,我们描述了如何利用已建立的非洲爪蟾命运图谱,通过对4细胞和8细胞胚胎的特定卵裂球进行显微注射,来靶向发育中的非洲爪蟾肾脏(前肾)。注射谱系示踪剂可验证注射的特异性靶向。胚胎发育到38 - 40期后,采用整体免疫染色来观察前肾发育情况,并评估靶向细胞对前肾的贡献。除了前肾之外,相同的技术还可用于靶向其他组织类型。

相似文献

1
Technique to Target Microinjection to the Developing Xenopus Kidney.
J Vis Exp. 2016 May 3(111):53799. doi: 10.3791/53799.
3
The Na+/PO4 cotransporter SLC20A1 gene labels distinct restricted subdomains of the developing pronephros in Xenopus and zebrafish embryos.
Gene Expr Patterns. 2006 Oct;6(7):667-72. doi: 10.1016/j.modgep.2006.01.005. Epub 2006 Mar 10.
4
A role for Xlim-1 in pronephros development in Xenopus laevis.
Dev Biol. 2000 Dec 15;228(2):256-69. doi: 10.1006/dbio.2000.9951.
5
Annexin IV (Xanx-4) has a functional role in the formation of pronephric tubules.
Development. 2002 Apr;129(7):1693-704. doi: 10.1242/dev.129.7.1693.
6
A functional screen for genes involved in Xenopus pronephros development.
Mech Dev. 2008 Jul;125(7):571-86. doi: 10.1016/j.mod.2008.03.001. Epub 2008 Mar 17.
7
Targeted microinjection of synthetic mRNAs to alter retina gene expression in Xenopus embryos.
Methods Mol Biol. 2012;884:91-111. doi: 10.1007/978-1-61779-848-1_6.
8
High-magnification in vivo imaging of Xenopus embryos for cell and developmental biology.
Cold Spring Harb Protoc. 2010 May;2010(5):pdb.prot5427. doi: 10.1101/pdb.prot5427.
9
A comparative study of cellular diversity between the Xenopus pronephric and mouse metanephric nephron.
Kidney Int. 2023 Jan;103(1):77-86. doi: 10.1016/j.kint.2022.07.027. Epub 2022 Aug 31.
10
Differential expression of arid5b isoforms in Xenopus laevis pronephros.
Int J Dev Biol. 2014;58(5):363-8. doi: 10.1387/ijdb.140029mu.

引用本文的文献

2
Tissue-Targeted CRISPR-Cas9-Mediated Genome Editing of Multiple Homeologs in F-Generation Embryos.
Cold Spring Harb Protoc. 2022 Mar 1;2022(3):pdb.prot107037. doi: 10.1101/pdb.prot107037.
3
The Wnt/PCP formin Daam1 drives cell-cell adhesion during nephron development.
Cell Rep. 2021 Jul 6;36(1):109340. doi: 10.1016/j.celrep.2021.109340.
4
Divergent roles of the Wnt/PCP Formin Daam1 in renal ciliogenesis.
PLoS One. 2019 Aug 30;14(8):e0221698. doi: 10.1371/journal.pone.0221698. eCollection 2019.
5
The Many Faces of : as a Model System to Study Wolf-Hirschhorn Syndrome.
Front Physiol. 2019 Jun 26;10:817. doi: 10.3389/fphys.2019.00817. eCollection 2019.
6
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.
Genet Med. 2019 Dec;21(12):2755-2764. doi: 10.1038/s41436-019-0576-0. Epub 2019 Jul 2.
7
Modeling congenital kidney diseases in .
Dis Model Mech. 2019 Apr 9;12(4):dmm038604. doi: 10.1242/dmm.038604.
8
Dynamin Binding Protein Is Required for Kidney Development.
Front Physiol. 2019 Feb 26;10:143. doi: 10.3389/fphys.2019.00143. eCollection 2019.
9
Transgenic Xenopus laevis Line for In Vivo Labeling of Nephrons within the Kidney.
Genes (Basel). 2018 Apr 6;9(4):197. doi: 10.3390/genes9040197.
10
Tissue-Specific Gene Inactivation in : Knockout of in the Kidney with CRISPR/Cas9.
Genetics. 2018 Feb;208(2):673-686. doi: 10.1534/genetics.117.300468. Epub 2017 Nov 29.

本文引用的文献

1
Xenbase, the Xenopus model organism database; new virtualized system, data types and genomes.
Nucleic Acids Res. 2015 Jan;43(Database issue):D756-63. doi: 10.1093/nar/gku956. Epub 2014 Oct 13.
3
Pronephric tubulogenesis requires Daam1-mediated planar cell polarity signaling.
J Am Soc Nephrol. 2011 Sep;22(9):1654-64. doi: 10.1681/ASN.2010101086. Epub 2011 Jul 29.
4
Requirement of Wnt/beta-catenin signaling in pronephric kidney development.
Mech Dev. 2009 Mar-Apr;126(3-4):142-59. doi: 10.1016/j.mod.2008.11.007. Epub 2008 Dec 7.
5
Organization of the pronephric kidney revealed by large-scale gene expression mapping.
Genome Biol. 2008;9(5):R84. doi: 10.1186/gb-2008-9-5-r84. Epub 2008 May 20.
8
The chloride conductance channel ClC-K is a specific marker for the Xenopus pronephric distal tubule and duct.
Gene Expr Patterns. 2003 Jun;3(3):347-50. doi: 10.1016/s1567-133x(03)00032-2.
9
The Xenopus pronephros as a model system for the study of kidney development and pathophysiology.
Nephrol Dial Transplant. 2002;17 Suppl 9:73-4. doi: 10.1093/ndt/17.suppl_9.73.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验